PEMer: a computational framework with simulation-based error models for inferring genomic structural variants from massive paired-end sequencing data

Overview of attention for article published in Genome Biology, February 2009

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So far, Dimensions has found 233 publications that cite this research output.

233

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Unravelling the Genetic Landscape of Hemiplegic Migraine: Exploring Innovative Strategies and Emerging Approaches

Article in Genes (March 2024)

The impact of FASTQ and alignment read order on structural variant calling from long-read sequencing data

Article in PeerJ (March 2024)

Incorporating CNV analysis improves the yield of exome sequencing for rare monogenic disorders—an important consideration for resource-constrained settings

Article in Frontiers in Genetics (December 2023)

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